Evidence map›Paper›PMID 30902072›Full record

ArticleBMC cancer2019

LUADpp: an effective prediction model on prognosis of lung adenocarcinomas based on somatic mutational features.

Jiaxian Yu, Yueming Hu, Yafei Xu, Jue Wang, Jiajie Kuang, Wei Zhang, Jianlin Shao, Dianjing Guo, Yejun Wang

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

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  5. Metabolic heterogeneity in early-stage lung adenocarcinoma revealed by RNA-seq and scRNA-seq.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Jiaxian YuDepartment of Cell Biology and Genetics, Shenzhen University Health Science Center, Shenzhen, 518060, China.
Yueming HuDepartment of Cell Biology and Genetics, Shenzhen University Health Science Center, Shenzhen, 518060, China.
Yafei XuDepartment of Cell Biology and Genetics, Shenzhen University Health Science Center, Shenzhen, 518060, China.
Jue WangState Key Laboratory of Agrobiotechnology and School of Life Science, The Chinese University of Hong Kong, Shatin, Hong Kong, China.
Jiajie KuangDepartment of Cell Biology and Genetics, Shenzhen University Health Science Center, Shenzhen, 518060, China.
Wei ZhangSehnzhen GenRead Technology Co., Ltd., Shenzhen, 518000, China.
Jianlin ShaoZhejiang Hospital, 12 Lingyin Rd, Hangzhou, 310003, China.
Dianjing GuoState Key Laboratory of Agrobiotechnology and School of Life Science, The Chinese University of Hong Kong, Shatin, Hong Kong, China. djguo@cuhk.edu.hk.
Yejun WangDepartment of Cell Biology and Genetics, Shenzhen University Health Science Center, Shenzhen, 518060, China. wangyj@szu.edu.cn.
Shenzhen University Health Science Center · CNChinese University of Hong Kong · CNZhejiang Hospital · CN

Funding

Guangdong Provincial Undergraduate Training Program for Innovation and Entrepreneurship 105902018118National Natural Science Foundation of China 81802705Natural Science Foundation of SZU 2015059Natural Science Funding of Shenzhen JCYJ20160422091914681Natural Science Funding of Shenzhen JCYJ201607115221141Special Fund for the Cultivation of Guangdong College Students' Scientific and Technological Innovation - Climbing Program pdjh2019b0420
6 · The paper itself

Abstract

backgroundLung adenocarcinoma is the most common type of lung cancers. Whole-genome sequencing studies disclosed the genomic landscape of lung adenocarcinomas. however, it remains unclear if the genetic alternations could guide prognosis prediction. Effective genetic markers and their based prediction models are also at a lack for prognosis evaluation.

methodsWe obtained the somatic mutation data and clinical data for 371 lung adenocarcinoma cases from The Cancer Genome Atlas. The cases were classified into two prognostic groups (3-year survival), and a comparison was performed between the groups for the somatic mutation frequencies of genes, followed by development of computational models to discrete the different prognosis.

resultsGenes were found with higher mutation rates in good (≥ 3-year survival) than in poor (< 3-year survival) prognosis group of lung adenocarcinoma patients. Genes participating in cell-cell adhesion and motility were significantly enriched in the top gene list with mutation rate difference between the good and poor prognosis group. Support Vector Machine models with the gene somatic mutation features could well predict prognosis, and the performance improved as feature size increased. An 85-gene model reached an average cross-validated accuracy of 81% and an Area Under the Curve (AUC) of 0.896 for the Receiver Operating Characteristic (ROC) curves. The model also exhibited good inter-stage prognosis prediction performance, with an average AUC of 0.846 for the ROC curves.

conclusionThe prognosis of lung adenocarcinomas is related with somatic gene mutations. The genetic markers could be used for prognosis prediction and furthermore provide guidance for personal medicine.

Indexed as

Models, BiologicalSupport Vector MachineAdenocarcinoma of LungBiomarkers, TumorComputational BiologyDatasets as TopicFeasibility StudiesGenomicsHumansLung NeoplasmsMutationPrecision MedicinePrognosisROC CurveSurvival AnalysisSurvival RateBiomarkers, TumorLung adenocarcinomasMachine learningPersonal medicineSomatic mutationalSupport vector machine model

Identifiers

PMID30902072
PMCPMC6431052
OpenAlexW2947792339

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.